
887579-62-6
- Product Name:5-cyanonicotinic acid
- Molecular Formula:C7H4N2O2
- Purity:99%
- Molecular Weight:148.12
Product Details
Purity:99%
Manufacturer Supply Best Quality 5-cyanonicotinic acid 887579-62-6 with Efficient Transportation
- Molecular Formula:C7H4N2O2
- Molecular Weight:148.12
- Vapor Pressure:0mmHg at 25°C
- Boiling Point:352.574°C at 760 mmHg
- Flash Point:167.031°C
- PSA:73.98000
- Density:1.425g/cm3
- LogP:0.65148
5-CYANO-3-PYRIDINECARBOXYLIC ACID(Cas 887579-62-6) Usage
InChI:InChI=1/C7H4N2O2/c8-2-5-1-6(7(10)11)4-9-3-5/h1,3-4H,(H,10,11)
887579-62-6 Relevant articles
COMPOUNDS AND METHODS for the inhibition of HDAC
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Paragraph 0151-0152, (2015/11/24)
Disclosed are compounds having the formu...
Discovery of tetrasubstituted imidazolines as potent and selective neuropeptide Y Y5 receptor antagonists: Reduced human ether-a-go-go related gene potassium channel binding affinity and potent antiobesity effect
Sato, Nagaaki,Ando, Makoto,Ishikawa, Shiho,Jitsuoka, Makoto,Nagai, Keita,Takahashi, Hirobumi,Sakuraba, Aya,Tsuge, Hiroyasu,Kitazawa, Hidefumi,Iwaasa, Hisashi,Mashiko, Satoshi,Gomori, Akira,Moriya, Ryuichi,Fujino, Naoko,Ohe, Tomoyuki,Ishihara, Akane,Kanatani, Akio,Fukami, Takehiro
supporting information; experimental part, p. 3385 - 3396 (2010/03/24)
A series of novel imidazoline derivative...
4,6-DISUBSTITUTED PYRIMIDINES AND THEIR USE AS PROTEIN KINASE INHIBITORS
-
Page/Page column 57, (2008/06/13)
The invention relates to novel pyrimidin...
Mandelic acid derivatives and their use as throbin inhibitors
-
Page/Page column 41, (2008/06/13)
There is provided a compound of formula ...
887579-62-6 Process route
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106726-82-3
3-Cyano-5-methoxycarbonylpyridine

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887579-62-6
5-cyano-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
With
water; lithium hydroxide;
In
tetrahydrofuran;
at 0 - 20 ℃;
for 1h;
|
78% |
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1158971-89-1
phenylmethyl 5-cyano-3-pyridinecarboxylate

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-
887579-62-6
5-cyano-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
With
palladium 10% on activated carbon; hydrogen;
In
methanol;
at 20 ℃;
under 760.051 Torr;
|
64% |
887579-62-6 Upstream products
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Nicotinic acid N-oxide
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sodium cyanide
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5-carbamoylpyridine-3-carboxylic acid
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phenylmethyl 5-cyano-3-pyridinecarboxylate
887579-62-6 Downstream products
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5-[(4S,5S)-4-(4-fluorophenyl)-4-(6-fluoro-3-pyridyl)-5-methyl-4,5-dihydro-1H-imidazol-2-yl]-3-pyridinecarbonitrile
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N-((4-(4-phenylthiazol-2-yl)tetrahydro-2H-pyran-4-yl)methyl)-5-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)nicotinamide
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N-(2-(2-(4-chlorophenyl)thiazol-4-yl)ethyl)-5-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)nicotinamide
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N-(2-(2-(4-chlorophenyl)thiazol-4-yl)-2-methylpropyl)-5-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)nicotinamide
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